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Building a detailed understanding of the structure function relationship is a crucial step in the optimization of molecular photocatalysts employed in water splitting schemes. The optically dark nature of their active sites usually prevents a complete mapping of the photoinduced dynamics. In this work, transient X-ray absorption spectroscopy highlights the electronic and geometric changes that affect such a center in a bimetallic model complex. Upon selective excitation of the ruthenium chromophore, the cobalt moiety is reduced through intramolecular electron transfer and undergoes a spin flip accompanied by an average bond elongation of 0.20 +/- 0.03 angstrom. The analysis is supported by simulations based on density functional theory structures (B3LYP*/TZVP) and FEFF 9.0 multiple scattering calculations. More generally, these results exemplify the large potential of the technique for tracking elusive intermediates that impart unique functionalities in photochemical devices.

Theoretical predictions show that depending on the populations of the Fe 3dxy, 3dxz, and 3dyz orbitals two possible quintet states can exist for the high-spin state of the photoswitchable model system [Fe(terpy)2]2+. The differences in the structure and molecular properties of these 5B2 and 5E quintets are very small and pose a substantial challenge for experiments to resolve them. Yet for a better understanding of the physics of this system, which can lead to the design of novel molecules with enhanced photoswitching performance, it is vital to determine which high-spin state is reached in the transitions that follow the light excitation. The quintet state can be prepared with a short laser pulse and can be studied with cutting-edge time-resolved X-ray techniques. Here we report on the application of an extended set of X-ray spectroscopy and scattering techniques applied to investigate the quintet state of [Fe(terpy)2]2+ 80 ps after light excitation. High-quality X-ray absorption, nonresonant emission, and resonant emission spectra as well as X-ray diffuse scattering data clearly reflect the formation of the high-spin state of the [Fe(terpy)2]2+ molecule; moreover, extended X-ray absorption fine structure spectroscopy resolves the Fe–ligand bond-length variations with unprecedented bond-length accuracy in time-resolved experiments. With ab initio calculations we determine why, in contrast to most related systems, one configurational mode is insufficient for the description of the low-spin (LS)–high-spin (HS) transition. We identify the electronic structure origin of the differences between the two possible quintet modes, and finally, we unambiguously identify the formed quintet state as 5E, in agreement with our theoretical expectations.

With the arrival of X-ray Free Electron Lasers (XFELs), 2D area detectors with a large dynamic range for detection of hard X-rays with fast readout rates are required for many types of experiments. Extracting the desired information from these detectors has been challenging due to unpredicted fluctuations in the measured images. For techniques such as time-resolved X-ray Diffuse Scattering (XDS), small differences in signal intensity are the starting point for analysis. Fluctuations in the total detected signal remain in the differences under investigation, obfuscating the signal. To correct such artefacts, Singular Value Decomposition (SVD) can be used to identify and characterize the observed detector fluctuations and assist in assigning some of them to variations in physical parameters such as X-ray energy and X-ray intensity. This paper presents a methodology for robustly identifying, separating and correcting fluctuations on area detectors based on XFEL beam characteristics, to enable the study of temporally resolved solution state chemistry on the femtosecond timescale.

Theoretical predictions show that depending on the populations of the Fe 3dxy, 3dxz, and 3dyz orbitals two possible quintet states can exist for the high-spin state of the photoswitchable model system [Fe(terpy)2]2+. The differences in the structure and molecular properties of these 5B2 and 5E quintets are very small and pose a substantial challenge for experiments to resolve them. Yet for a better understanding of the physics of this system, which can lead to the design of novel molecules with enhanced photoswitching performance, it is vital to determine which high-spin state is reached in the transitions that follow the light excitation. The quintet state can be prepared with a short laser pulse and can be studied with cutting-edge time-resolved X-ray techniques. Here we report on the application of an extended set of X-ray spectroscopy and scattering techniques applied to investigate the quintet state of [Fe(terpy)2]2+ 80 ps after light excitation. High-quality X-ray absorption, nonresonant emission, and resonant emission spectra as well as X-ray diffuse scattering data clearly reflect the formation of the high-spin state of the [Fe(terpy)2]2+ molecule; moreover, extended X-ray absorption fine structure spectroscopy resolves the Fe–ligand bond-length variations with unprecedented bond-length accuracy in time-resolved experiments. With ab initio calculations we determine why, in contrast to most related systems, one configurational mode is insufficient for the description of the low-spin (LS)–high-spin (HS) transition. We identify the electronic structure origin of the differences between the two possible quintet modes, and finally, we unambiguously identify the formed quintet state as 5E, in agreement with our theoretical expectations.

Summary By combining a synchrotron X-ray source and the microtomography technique, the displacement gradient tensor components can be measured directly throughout the volume of a metal sample containing highly absorbing marker particles to detect material flow. The present article describes application of these techniques to compression of a rectangular Al–W specimen with a central hole. The results show that the externally imposed axial displacement gradient is accommodated mainly in two 45° shear bands passing through the hole. A simple deformation analysis provides insight into shear band formation.

Newly developed experimental methods allow the extension of surface strain measurements into three dimensions throughout the bulk of opaque materials. By comparing two specimens with different geometries but consisting of similar materials under compression deformation, the ability of one of these new methods to distinguish between homogeneous and heterogeneous response to identical macroscopic boundary conditions is illustrated. Extending a previous study of a specimen deforming homogeneously to the entire specimen volume rather than a small subvolume, the effect of the marker particles on the material properties is discussed.

Ultrafast structural dynamics of the metal to ligand charge transfer (MLCT) states of two copper bis-phenanthroline complexes were captured by using x-ray transient absorption (XTA) spectroscopy at the Linac Coherent Light Source and further described by theoretical calculations. These complexes have the general formula [Cu(I)(R)_2]+, where R = 2,9-dimethyl-1,10-phenanthroline (dmp) and 2,9-diphenyl-1,10-phenanthroline disulfonic acid disodium salt (dpps). [Cu(I)(dmp)_2]+ has methyl groups at the 2,9 positions of phenanthroline (phen) and adopts a pseudo-tetrahedral geometry. In contrast, [Cu(I)(dpps)_2]+ possesses two bulky phenyl-sulfonate groups attached to each phen ligand that force the molecule to adopt a flattened tetrahedral geometry in the ground state. Previously, optical transient absorption (OTA) and synchrotron based XTA experiments with 100 ps time resolution have been employed to study the relationship between structural distortions and excited state relaxation pathways in the two complexes. However, the dynamics of the MLCT transition during the first few picoseconds after excitation in these complexes remained unclear because of limitations in element specificity in OTA and in the time resolution of synchrotron sources in XTA. In this experiment, the local coordination geometry and oxidation state of copper were probed with a temporal resolution of ~300 fs. Unexpectedly, the depletion of the Cu(I) signal due to the MLCT transition was found to be non-impulsive in the case of [Cu(I)(dpps)_2]+ with a time constant of 0.6 ps, while the Cu(I) depletion in [Cu(I)(dmp)_2]+ was instantaneous within the 300 fs instrument response time. The slower Cu(I) depletion kinetics in [Cu(I)(dpps)_2]+, previously unobserved in femtosecond OTA experiments, is likely due to intramolecular motions on the sub-picosecond time scale that could alter the localization of the transferred electron in the phen ligands.

The development of new X-ray light sources, XFELs, with unprecedented time and brilliance characteristics has led to the availability of very large datasets with high time resolution and superior signal strength. The chaotic nature of the emission processes in such sources as well as entirely novel detector demands has also led to significant challenges in terms of data analysis. This paper describes a heuristic approach to datasets where spurious background contributions of a magnitude similar to (or larger) than the signal of interest prevents conventional analysis approaches. The method relies on singular-value decomposition of no-signal subsets of acquired datasets in combination with model inputs and appears generally applicable to time-resolved X-ray diffuse scattering experiments.

Within the last decade, significant advances in X-ray sources and instrumentation as well as simultaneous developments in analysis methodology has allowed the field of fast- and ultrafast time-resolved X-ray studies of solution-state systems to truly come of age. We here describe some aspects of the physics involved as well as the experimental methodology that have facilitated this development. Building on this foundation, we discuss how the information-poor, but time-resolved (difference) scattering signals can be analyzed in a quantitative model-comparison framework to provide robust information on sub-Angstrom structural changes taking place on femtosecond to nanosecond time scales. We illustrate this approach by a presentation of recent results from the Centre for Molecular Movies at the Technical University of Denmark.

International audience; X-ray free electron lasers (XFELs) deliver short (

WOS:000323520600021; International audience; In time-resolved laser pump, X-ray probe wide-angle X-ray scattering experiments on systems in solution the structural response of the system is accompanied by a solvent response. The solvent response is caused by reorganization of the bulk solvent following the laser pump event, and in order to extract the structural information of the solute, the solvent response has to be treated. Methodologies capable of doing so include both theoretical modelling and experimental determination of the solvent response. In the work presented here, we have investigated how to obtain a reproducible solvent response-the solvent term-experimentally when applying laser pump, X-ray probe time-resolved wide-angle X-ray scattering. The solvent term describes difference scattering arising from the structural response of the solvent to changes in the hydrodynamic parameters: pressure, temperature and density. We present results based on NIR and dye mediated solvent heating, and demonstrate that the solvent response is independent of the heating method. The NIR heating is shown to be rendered unusable by higher order effects under certain experimental conditions, while the dye mediated solvent heating is demonstrated to exhibit first order behaviour with respect to the amount of energy deposited in the solution. We introduce a standardized method for recording solvent responses in laser pump, X-ray probe time-resolved X-ray wide-angle scattering experiments by using dye mediated solvent heating. Furthermore, we have generated a library of solvent terms, which can be used to describe the solvent term in any TRWAXS experiment, and made it available online.

We report on extending hard X-ray emission spectroscopy (XES) along with resonant inelastic X-ray scattering (RIXS) to study ultrafast phenomena in a pump-probe scheme at MHz repetition rates. The investigated systems include low-spin (LS) Fe-II complex compounds, where optical pulses induce a spin-state transition to their (sub)nanosecond-lived high-spin (HS) state. Time-resolved XES clearly reflects the spin-state variations with very high signal-to-noise ratio, in agreement with HS-LS difference spectra measured at thermal spin crossover, and reference HS-LS systems in static experiments, next to multiplet calculations. The 1s2p RIXS, measured at the Fe Is pre-edge region, shows variations after laser excitation, which are consistent with the formation of the HS state. Our results demonstrate that X-ray spectroscopy experiments with overall rather weak signals, such as RIXS, can now be reliably exploited to study chemical and physical transformations on ultrafast time scales. (C) 2012 Elsevier B.V. All rights reserved. (Less)

Ground- and excited-state structures of the bimetallic, ligand-bridged compound Ir2(dimen)4(2+) are investigated in acetonitrile by means of time-resolved X-ray scattering. Following excitation by 2 ps laser pulses at 390 nm, analysis of difference scattering patterns obtained at eight different time delays from 250 ps to 300 ns yields a triplet excited-state distance between the two Ir atoms of 2.90(2) Å and a triplet excited-state lifetime of 410(70) ns. A model incorporating the presence of two ground-state structures differing in Ir–Ir separation is demonstrated to fit the obtained data very well, in agreement with previous spectroscopic investigations. Two ground-state isomers with Ir–Ir separations of 3.60(9) and 4.3(1) Å are found to contribute equally to the difference scattering signal at short time delays. Further studies demonstrate the feasibility of increasing the effective time resolution from the 100 ps probe width down to the 10 ps regime by positioning the laser pump pulse at selected points in the X-ray probe pulse. This approach is used to investigate the structures of both the singlet and the triplet excited states of Ir2(dimen)4(2+).

The present communication describes the identification and structural characterization of a photo-induced transient trinuclear Ag–Pt–Pt complex, in which a pronounced internal structural change of the excited-state PtPOP moiety is observed upon complexation with the Ag ion.

As ultrafast time-resolved studies of liquid systems with the laser pump/X-ray scattering probe method have come of age over the past decade, several groups have developed methods for the analysis of such X-ray scattering data. The present article describes a method developed primarily with a focus on determining structural parameters in the excited states of medium-sized molecules (~30 atoms) in solution. The general methodology is set in a maximum-likelihood framework and is introduced through the analysis of the photoactive platinum compound PtPOP, in particular the structure of its lowest triplet excited state (3A2u). Emphasis is put on structure determination in terms of model comparisons and on the information content of difference scattering signals as well as the related experimental variables. Several suggestions for improving the accuracy of these types of measurements are presented.

We propose and describe a microfluidic system for high intensity x-ray measurements. The required open access to a microfluidic channel is provided by an out-of-plane capillary burst valve (CBV). The functionality of the out-of-plane CBV is characterized with respect to the diameter of the windowless access hole, ranging from 10 to 130 Am. Maximum driving pressures from 22 to 280 mbar corresponding to refresh rates of the exposed sample from 300 Hz to 54 kHz is demonstrated. The microfluidic system is tested at beamline ID09b at the ESRF synchrotron radiation facility in Grenoble, and x-ray scattering measurements are shown to be feasible and to require only very limited amounts of sample

The recent developments in X-ray detectors have opened new possibilities in the area of time-resolved pump/probe X-ray experiments; this article presents the novel use of a PILATUS detector to achieve X-ray pulse duration limited time-resolution at the Advanced Photon Source (APS), USA. The capability of the gated PILATUS detector to selectively detect the signal from a given X-ray pulse in 24 bunch mode at the APS storage ring is demonstrated. A test experiment performed on polycrystalline organic thin films of alpha-perylene illustrates the possibility of reaching an X-ray pulse duration limited time-resolution of 60 ps using the gated PILATUS detector. This is the first demonstration of X-ray pulse duration limited data recorded using an area detector without the use of a mechanical chopper array at the beamline.

A recently developed marker-based technique for mapping of the displacement gradient tensor and the strain throughout the bulk of optically opaque specimens is presented and applied to an aluminium alloy multicrystal. Through investigations at 4%, 10% and 14% axial strains, the internal strain field is observed to be non-homogenous with the observed patterns present throughout the range of strains investigated. The morphology of the strain field is visualized with a resolution better than 50μm and variations are tentatively associated with the grain structure as recorded by EBSD. Future applications of the technique in combination with other 3-dimensional approaches are discussed with respect to comparison with Finite Element modelling approaches.

We derive a formulation for evaluating (time-resolved) x-ray scattering signals of solvated chemical systems, based on pairwise radial distribution functions, with the aim of this formulation to accompany molecular dynamics simulations. The derivation is described in detail to eliminate any possible ambiguities, and the result includes a modification to the atom-type formulation which to our knowledge is previously unaccounted for. The formulation is numerically implemented and validated.

Understanding the distributions of strain within solid bodies undergoing plastic deformations has been of interest for many years in a wide range of disciplines, ranging from basic materials science to biology. However, the desire to investigate these strain fields has been frustrated by the inaccessibility of the interior of most samples to detailed investigation without destroying the sample in the process. To some extent, this has been remedied by the development of advanced surface measurement techniques as well as computer models based on Finite Element methods. Over the last decade, this situation has changed by the introduction of a range of tomographic methods based both on advances in computer technology and in instrumentation, advances which have opened up the interior of optically opaque samples for detailed investigations. We present a general method for assessing the strain in the interior of marker-containing specimens undergoing various types of deformation. The results are compared with Finite Element modelling.

A method for non-destructive characterization of plastic deformation in bulk materials is presented. The method is based on X-ray absorption microtomography investigations using X-rays from a synchrotron source. The method can be applied to materials that contain marker particles, which have an atomic number significantly different from that of the matrix material. Data were acquired at the dedicated microtomography instrument at beamline BW2 at HASYLAB/DESY, for a cylindrical aluminium sample containing W particles with an average particle diameter of 7 μm. The minimum detectable size of the maker particles is 1-2 μm with the present spatial resolution at HASYLAB. The position (x,y,z) of all the detected marker particles within 1 mm 3 was determined as function of strain. The sample was deformed in stepwise compression along the axis of the cylinder. A tomographic scan was performed after each deformation step. After a series of image analysis steps to identify the centre of mass of individual particles and alignment of the successive tomographic reconstructions, the displacements of individual particles could be tracked as a function of external strain. The particle displacements are then used to identify local displacement gradient components, from which the local 3D plastic strain tensor can be determined. This allows us to map the strain components as a function of location inside a deforming metallic solid.

Photovoltaic processesof the earth abundant and non-toxic Cu2ZnSnS4 (CZTS) absorbermaterial in 3. generation solar cells can be investigated by time resolved X-ray absorptionspectroscopy (TR-XAS) using a synchrotron-based X-ray source and synchronizedlaser excitation (pump-probe method). Such experiments require high qualityCZTS [1] stabilized as a nanoparticle (NP) ink as a model system, which is alsoapplicable for low-cost up-scalable roll-to-roll (R2R) printing.